MEDICOR QUALITY CONTROL BUFFER— 510(k) K791287

Name: FDA 510(k) clearance K791287
Creator: U.S. Food and Drug Administration
Published: 1979-08-16

Substantially Equivalent

Medicor USA , Ltd.

FDA 510(k) clearance K791287 for MEDICOR QUALITY CONTROL BUFFER, Substantially Equivalent on 1979-08-16. Applicant: Medicor USA , Ltd.. Device class: 1.

Clearance details

Applicant: Medicor USA , Ltd.
Product code: Code JJS
Device class: Class 1
Regulation: 21 CFR 862.1660
Advisory panel: Clinical Chemistry
Date received: 1979-07-10
Decision date: 1979-08-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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